OSC2824 AND nstd224 - dbVar - NCBI

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Number of Variants: 9

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6625576	copy number variation	3	nstd224	human		GRCh37 chr1: 12,907,683-12,921,254 , GRCh38.p12 chr1: 12,847,830-12,861,399 , GRCh38.p12 chr1\|NW_012132914.1: 29,343-42,912	PRAMEF2, HNRNPCL1
nsv6628116	copy number variation	277	nstd224	human		GRCh37 chr2: 38,956,836-38,972,328 , GRCh38.p12 chr2: 38,729,694-38,745,186	SRSF7, GALM
nsv6626817	copy number variation	29	nstd224	human		GRCh37 chr21: 14,669,931-14,844,368 , GRCh38.p12 chr21: 13,297,610-13,472,047	GTF2IP2, MIR3156-3, 2 more genes
nsv6629867	copy number variation	3	nstd224	human		GRCh37 chr4: 410,015-438,080 , GRCh38.p12 chr4: 416,226-444,291	LOC100533734, ABCA11P, 1 more genes
nsv6621655	copy number variation	8	nstd224	human		GRCh37 chr13: 19,121,950-19,263,735 , GRCh38.p12 chr13: 18,547,810-18,689,595	TERF1P5, FEM1AP4, 1 more genes
nsv6627055	copy number variation	71	nstd224	human		GRCh37 chr22: 18,892,575-19,008,108 , GRCh38.p12 chr22: 18,905,062-19,020,595	DGCR6, PRODH, 1 more genes
nsv6624242	copy number variation	42	nstd224	human		GRCh37 chr17: 44,187,257-44,293,020 , GRCh38.p12 chr17: 46,109,891-46,215,654 , GRCh38.p12 chr17\|NT_187663.1: 811,990-917,827	LOC107985027, KANSL1-AS1, 1 more genes
nsv6630307	copy number variation	74	nstd224	human		GRCh37 chr5: 140,223,194-140,238,124 , GRCh38.p12 chr5: 140,843,609-140,858,539	PCDHA7, PCDHA4, 9 more genes
nsv6622829	copy number variation	3	nstd224	human		GRCh37 chr15: 22,368,936-22,468,503 , GRCh38.p12 chr15: 22,080,985-22,180,552	OR4N4, RPS8P10, 6 more genes

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